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Grouped Pigmentation of the Macula (DOID:9005303)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
retinal disease +     
acanthosis nigricans +   
achromatopsia 4  
Achromatopsia 5  
Acrootoocular Syndrome 
ADULT syndrome  
Aicardi syndrome 
Al Gazali Sabrinathan Nair Syndrome 
Alacrima +   
Albinism +   
angioid streaks +  
aniridia +   
Anonychia with Flexural Pigmentation 
ataxia with oculomotor apraxia type 3  
Ataxia-Microcephaly-Cataract Syndrome 
Ataxia-Oculomotor Apraxia 4  
Ausems Wittebol-Post Hennekam Syndrome 
BADS syndrome 
basal laminar drusen  
Basaran Yilmaz Syndrome  
Bietti crystalline corneoretinal dystrophy  
Bloch-Sulzberger syndrome +   
Bothnia retinal dystrophy  
Bullous Dystrophy, Hereditary Macular Type 
Cafe-au-Lait Spots +   
cataract 17 multiple types  
cataract 22 multiple types  
cataract 35 
Cataract, Floriform 
Cataract, Pulverulent 
Cavitary Optic Disc Anomalies  
Central Serous Chorioretinopathy  
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
Cholestasis with Gallstone, Ataxia, and Visual Disturbance 
chorioretinal scar +  
Choroideremia +   
cone dystrophy +   
cone-rod dystrophy +   
Congenital Alacrima +   
Congenital Fibrosis of Extraocular Muscles, 2  
Congenital Fibrosis of Extraocular Muscles, 3A, with or without Extraocular Involvement  
Congenital Fibrosis of Extraocular Muscles, 3B  
Congenital Fibrosis of Extraocular Muscles, 3C 
Congenital Fibrosis of Extraocular Muscles, 5  
Congenital Mydriasis +   
conjunctival pigmentation 
Cornea Plana 1 
Cornea Plana 2  
corneal dystrophy +   
diabetic retinopathy +   
Duane retraction syndrome +   
dyschromatosis symmetrica hereditaria  
dyschromatosis universalis hereditaria +   
Elejalde Disease 
enhanced S-cone syndrome  
Fleck Retina, Familial Benign  
FLOTCH Syndrome 
Foveal Hypoplasia with Anterior Segment Anomalies  
fundus albipunctatus  
Glaucoma 1, Open Angle, P  
Graves Ophthalmopathy  
Graying of Hair, Precocious 
Griscelli syndrome +   
Grouped Pigmentation of the Macula 
gyrate atrophy +   
hereditary night blindness +   
Hereditary Optic Atrophies +   
Heterochromia Iridis  
high hyperopia  
Histiocytic Dermatoarthritis 
Hyperpigmentation +   
hypertensive retinopathy  
Hypopigmentation +   
hypopigmentation of eyelid 
Iris Hypoplasia and Glaucoma  
Iris Pigment Epithelium Anomalies 
Isolated Foveal Hypoplasia 
Joubert syndrome 8  
Leber congenital amaurosis +   
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Macular Dystrophy, X-Linked +   
Macules Hereditary Congenital Hypopigmented and Hyperpigmented 
megalocornea +   
microcephaly and chorioretinopathy 1 +   
Microcephaly with Chorioretinopathy, Autosomal Dominant 
neonatal jaundice +   
nerve fibre bundle defect 
night blindness +   
Oculocerebral Hypopigmentation Syndrome Type Preus 
Oculomelic Amyoplasia  
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects 
Ophthalmomandibulomelic Dysplasia 
Peripapillary Atrophy, Beta Type 
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive  
Pigmented Paravenous Chorioretinal Atrophy  
Pigmented Purpuric Eruption 
preretinal fibrosis  
proliferative vitreoretinopathy +   
Radial Drusen, Autosomal Dominant 
Rambaud Galian Syndrome 
Ramos Arroyo Clark Syndrome 
Red Skin Pigment Anomaly of New Guinea 
renal hypomagnesemia 5 with ocular involvement  
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Retina Reperfusion Injury  
Retinal Aplasia 
Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis  
Retinal Arteries, Tortuosity of  
retinal artery occlusion +   
retinal degeneration +   
retinal detachment +   
Retinal Dysplasia +   
Retinal Dystrophy, Early Onset Severe  
retinal edema +   
Retinal Hemorrhage +   
retinal ischemia  
Retinal Neoplasms +   
Retinal Neovascularization  
retinal perforation +  
retinal vascular disease +   
retinal vasculitis +   
Retinal Vasculopathy with Cerebral Leukodystrophy  
retinitis +   
retinitis pigmentosa +   
Retinohepatoendocrinologic Syndrome 
retinopathy of prematurity +   
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
Roifman Syndrome  
rubeosis iridis 
Russell-Silver Syndrome, X-Linked 
Sickle Cell Retinopathy  
Skin/Hair/Eye Pigmentation, Variation In, 1  
Skin/Hair/Eye Pigmentation, Variation In, 10  
Skin/Hair/Eye Pigmentation, Variation In, 11  
Skin/Hair/Eye Pigmentation, Variation In, 4  
Skin/Hair/Eye Pigmentation, Variation In, 5  
Skin/Hair/Eye Pigmentation, Variation In, 6  
Skin/Hair/Eye Pigmentation, Variation In, 7  
Skin/Hair/Eye Pigmentation, Variation In, 8  
Skin/Hair/Eye Pigmentation, Variation In, 9  
Spondyloocular Syndrome, Autosomal Recessive  
Stickler Syndrome, Type I, Nonsyndromic Ocular  
stromal corneal pigmentation 
Symmetric Acroleukopathy 
Tang Hsi Ryu Syndrome 
Terminal Osseous Dysplasia and Pigmentary Defects  
Thumb Deformity, Alopecia, Pigmentation Anomaly 
urticaria pigmentosa  
Vascular Hyalinosis 
vitelliform macular dystrophy +   
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
Waardenburg Syndrome Type 4 +   
Walker-Warburg syndrome +   
Weill-Marchesani syndrome +   
White Forelock with Malformations 
Whyte Murphy Syndrome 
xeroderma pigmentosum +   
yellow nail syndrome +  

Exact Synonyms: Grouped Pigmentation of Retinal Pigment Epithelium
Primary IDs: MESH:C565530 ;   RDO:0014138

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